Other
Consistent with the company's policy of public data disclosure, this clinical trial results section includes result summaries of completed Lilly-sponsored clinical studies conducted on Lilly marketed products since July 1, 2004. The results of all Phase I, II, and III trials conducted in support of a product’s initial registration will be disclosed regardless of outcome, no later than when the first indication is approved and the drug is commercially available for patient use anywhere in the world. The results of all subsequent Phase II, III, and IV trials conducted after initial approval will be similarly disclosed within one year of trial completion. A trial’s results, irrespective of study phase, will be disclosed as soon as possible if there are significant safety findings.
Consistent with ICH E3 guidelines, Lilly will disclose the results of primary and secondary outcome measures that are specified in the study protocol, as well as additional safety and efficacy results that impact patient care and the use of our products. Also, Lilly discloses a comprehensive description of the trial design and methodology for each study. Results will be disclosed regardless of whether they support the hypothesis being tested or are contrary to the predicted outcome. Clinical trial results will be publicly disclosed as stated above, unless posting would compromise publication in a peer reviewed medical journal or contravene national laws or regulations. Results of studies that are under review by peer-reviewed journals that prohibit pre-publication disclosure will be posted on the registry at the time of publication. Clinical trial results are also disclosed through presentations and abstract submissions at professional scientific meetings.
The registry is also populated with the results of core efficacy and safety registration trials for products first approved after July 1, 1994.
Included are trial result summaries that are completed to date. The company will continue to disclose additional summaries and publication citations as they become available.
Summaries of clinical study results are intended to report the results of the study that were known at the time of each study's completion. The information contained in these summaries is not intended to promote or otherwise commercialize (directly or indirectly) any off-label or unapproved uses of Lilly medicines, nor is it intended to provide a comprehensive analysis of all data currently available regarding a particular drug. In some cases, more current information regarding a drug, including post-hoc analyses and meta-analyses, may be available as part of the general body of scientific knowledge in forms such as manuscripts, abstracts, or posters.
Clinical studies on Lilly products may also be sponsored and reported by
parties other than Lilly
in other clinical trial registries.
Trial Results
The following trials have been conducted for products in other therapeutic areas.
| Drug |
Disease |
Trial ID |
Trial Title |
Trial
Phase |
| Cialis for Benign Prostatic Hyperplasia |
Cialis |
Benign Prostatic Hyperplasia |
9120 |
A Multicenter, Parallel-Arm, Placebo-Controlled, Double-Blind Study to Evaluate the Efficacy and Safety of Tadalafil Administered Once Daily to Men with Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia |
2 |
| Cialis for Hypertension |
Cialis |
Hypertension |
10077 |
A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy and Safety of Tadalafil (5 mg and 20 mg) Administered Once Daily to Subjects with Mild to Moderate Hypertension |
2 |
| Cymbalta for Fibromyalgia |
Cymbalta |
Fibromyalgia |
6158 |
Duloxetine versus Placebo in the Treatment of Fibromyalgia Patients with or without Major Depressive Disorder |
3 |
Cymbalta |
Fibromyalgia |
6222 |
Dose Response Study of Duloxetine Versus Placebo in the Treatment of Fibromyalgia Syndrome |
3 |
Cymbalta |
Fibromyalgia |
9072 |
Duloxetine 60/120mg versus Placebo in the Treatment of Fibromyalgia |
3 |
Cymbalta |
Fibromyalgia |
9075 |
A 1-Year Safety Study of Duloxetine in Patients with Fibromyalgia |
3 |
| Xigris for Severe Sepsis |
Xigris |
Severe Sepsis |
1678 |
A Phase 3 Study to Determine the Efficacy and Safety for Recombinant Human Activated Protein C in Severe Sepsis |
3 |
Xigris |
Severe Sepsis |
6716 |
Investigation of the Efficacy and Safety of Drotrecogin Alfa (Activated) in Pediatric Severe Sepsis |
3 |
Xigris |
Severe Sepsis |
5771 |
Long-Term Follow-Up of Survivors from the PROWESS Trial (An Observational Study) |
3b |
Xigris |
Severe Sepsis |
6001 |
A Phase IIIb Study to Determine Efficacy and Safety of Extended Drotrecogin Alfa (Activated) Therapy in Patients with Persistent Requirement for Vasopressor Support After 96-Hour Infusion with Commercial Drotrecogin Alfa (Activated) |
3b |
Xigris |
Severe Sepsis |
6416 |
A Safety Evaluation Of Xigris [Drotrecogin Alfa (Activated)] In Hematoapoietic Stem Cell Transplant Patients With Severe Sepsis |
3b |
Xigris |
Severe Sepsis |
6669 |
Efficacy and Safety of Drotrecogin Alfa (activated) in Adult Patients with Early Stage Severe Sepsis
|
3b |
Xigris |
Severe Sepsis |
7252 |
Efficacy and Safety of Drotrecogin Alfa (activated) in Adult Patients with Early Stage Severe Sepsis
|
3b |
Xigris |
Severe Sepsis |
5502 |
An Open Label Study Of Drotrecogin Alfa (Activated) (LY203638) in Severe Sepsis |
3 / 4 |
Xigris |
Severe Sepsis |
7159 |
An Open Label Study Of Drotrecogin Alfa (Activated) In Adult Patients With Severe Sepsis And Multiple Organ Dysfunctions: A Phase IV Protocol
|
4 |
Xigris |
Severe Sepsis |
6009 |
The Pharmacokinetics of Xigris® [Drotrecogin Alfa (Activated)] in Patients =160 kg with Severe Sepsis
|
4 |
Xigris |
Severe Sepsis |
6743 |
A Randomized, Double-Blind, Placebo-Controlled Trial of Prophylactic Heparin in Patients with Severe Sepsis and Higher Disease Severity Who Are Undergoing Treatment with Drotrecogin Alfa (Activated)
|
4 |
| Yentreve: Clinical Pharmacology Study |
Yentreve |
Clinical Pharmacology Study |
6867 |
A Placebo-Controlled Study of Electrophysiological Effects of Supratherapeutic Doses of Duloxetine on the QT Interval |
1 |
| Yentreve for Stress Urinary Incontinence |
Yentreve |
Stress Urinary Incontinence
|
1129
|
Duloxetine for Urinary Incontinence: A Multiple-Dose Study for Efficacy and Safety
|
2 |
Yentreve |
Stress Urinary Incontinence
|
1604
|
Duloxetine Versus Placebo in the Relief of Stress Incontinence
|
2 |
Yentreve |
Stress Urinary Incontinence
|
2595a
|
Biomechanical Effects of Duloxetine on Bladder Function and Sphincter Resistance During the Emptying Phase and on Urethral Cycle Function in Women with Pure Genuine Stress Incontinence
|
2 |
Yentreve |
Stress Urinary Incontinence
|
2595b
|
Biomechanical Effects of Duloxetine on Bladder Function and Sphincter Resistance During the Emptying Phase and on Urethral Function During the Filling Phase of the Micturition Cycle in Women with Pure Genuine Stress Incontinence
|
2 |
Yentreve |
Stress Urinary Incontinence
|
2615a
|
Efficacy and Safety of Duloxetine compared with Placebo, Pelvic Floor Muscle Training, and Combined Duloxetine/Pelvic Floor Muscle Training in Subjects with Moderate to Severe Stress Urinary Incontinence
|
2 |
Yentreve |
Stress Urinary Incontinence
|
2615b
|
Efficacy and Safety of Duloxetine compared with Placebo, Pelvic Floor Muscle Training, and Combined Duloxetine/Pelvic Floor Muscle Training in Subjects with Moderate to Severe Stress Urinary Incontinence
|
2 |
Yentreve |
Stress Urinary Incontinence
|
2624a
|
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects Electing Surgery for Severe Pure Genuine Stress Incontinence
|
2 |
Yentreve |
Stress Urinary Incontinence
|
2624b
|
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects Electing Surgery for Severe Pure Genuine Stress Incontinence
|
2 |
Yentreve |
Stress Urinary Incontinence
|
5308
|
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Symptoms of Bladder Overactivity Due to Pure Detrusor Instability or Sensory Urgency
|
2 |
Yentreve |
Stress Urinary Incontinence
|
6984 |
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Bladder Overactivity |
2 |
Yentreve |
Stress Urinary Incontinence
|
2685
|
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
|
3 |
Yentreve |
Stress Urinary Incontinence
|
2686
|
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Stress Urinary Incontinence
|
3 |
Yentreve |
Stress Urinary Incontinence
|
2687
|
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
|
3 |
Yentreve |
Stress Urinary Incontinence
|
2688
|
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Stress Urinary Incontinence
|
3 |
Yentreve |
Stress Urinary Incontinence |
2689
|
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
|
3 |
Yentreve |
Stress Urinary Incontinence |
2690
|
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Stress Urinary Incontinence
|
3 |
Yentreve |
Stress Urinary Incontinence |
3171 |
Prospective Outcomes of Duloxetine in Usual Naturalistic Care in Women with Stress Urinary Incontinence |
3 |
Yentreve |
Stress Urinary Incontinence |
5309 |
Long-Term Monitoring of Safety in Subjects Treated with Duloxetine for Stress Urinary Incontinence
|
3 |
Yentreve |
Stress Urinary Incontinence |
6231 |
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence
|
3 |
Yentreve |
Stress Urinary Incontinence |
6232 |
Efficacy and Safety of Duloxetine Compared with Placebo in Subjects with Stress Urinary Incontinence |
3 |
Yentreve |
Stress Urinary Incontinence |
6192a |
Efficacy and Safety of Duloxetine Compared with Placebo in Women with Symptoms of
Mixed Urinary Incontinence |
3B |
Yentreve |
Stress Urinary Incontinence |
6192b |
Efficacy and Safety of Duloxetine Compared with Placebo in Women with Symptoms of
Mixed Urinary Incontinence |
3B |
Yentreve |
Stress Urinary Incontinence |
6195a |
The Effectiveness of Duloxetine Compared with Placebo in the Treatment of Predominant Stress Urinary Incontinence |
3B |
Yentreve |
Stress Urinary Incontinence |
6195b |
The Effectiveness of Duloxetine Compared with Placebo in the Treatment of Predominant Stress Urinary Incontinence |
3B |
Yentreve |
Stress Urinary Incontinence |
8049 |
The Safety and Effectiveness of Duloxetine Compared with Placebo and its Long-term
Safety and Efficacy in the Treatment of Predominant Stress Urinary Incontinence. |
3B |
Yentreve |
Stress Urinary Incontinence |
9587 |
Effect of Duloxetine on Valsalva Leak Point Pressure and Quantitative Rhabdosphincter Electromyography Measures in Women with Stress Urinary Incontinence
|
3B |
Yentreve |
Stress Urinary Incontinence |
8363 |
Study of Duloxetine HCl in Women of Different Demographic Characteristics and Comorbidities with Stress Urinary Incontinence: Evaluation of Efficacy and Safety
|
4 |
Yentreve |
Stress Urinary Incontinence |
8672 |
Duloxetine versus Placebo in the Treatment of Community-Dwelling Women Aged 65 Years or Older with Stress or Stress-Predominant Mixed Urinary Incontinence
|
4 |
|